Electrode plate, electrochemical apparatus, battery module, battery pack, and device

ABSTRACT

This application relates to the battery field, and specifically, to an electrode plate, an electrochemical apparatus, a battery module, a battery pack, and a device. The electrode plate in this application includes a current collector and an electrode active material layer disposed on at least one surface of the current collector, where the current collector includes a support layer and a conductive layer disposed on at least one surface of the support layer, a single-side thickness D2 of the conductive layer satisfies 30 nm≤D2≤3 μm, and a conductive primer layer including a conductive material and a bonding agent is further disposed between the current collector and the electrode active material layer. The electrode plate in this application has good machinability. An electrochemical apparatus including the electrode plate has high energy density, good electrical performance, and long-term reliability.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of PCT Patent Application No. PCT/CN2019/117143, entitled “ELECTRODE PLATE, ELECTROCHEMICAL APPARATUS, BATTERY MODULE, BATTERY PACK, AND DEVICE” filed on Nov. 11, 2019, which claims priority to Chinese Patent Application No. 201811638645.2, filed with the State Intellectual Property Office of the People's Republic of China on Dec. 29, 2018, and entitled “ELECTRODE PLATE, ELECTROCHEMICAL APPARATUS, BATTERY MODULE, BATTERY PACK, AND DEVICE”, all of which are incorporated herein by reference in their entirety.

TECHNICAL FIELD

This application relates to the battery field, and specifically, to an electrode plate, an electrochemical apparatus, a battery module, a battery pack, and a device.

BACKGROUND

Lithium-ion batteries have advantages such as high energy density, high output power, long cycle life, and low environmental pollution, and therefore are extensively applied in electric vehicles and consumer electronic products. As the application scope of the lithium-ion batteries is continuously expanded, people have higher requirements on mass energy density and volume energy density of the lithium-ion batteries.

To obtain a lithium-ion battery with high mass energy density and volume energy density, the following improvements are generally made to the lithium-ion battery: (1) selecting a positive electrode material or a negative electrode material with a high specific discharge capacity; (2) optimizing a mechanical design of the lithium-ion battery to minimize a volume of the lithium-ion battery; (3) selecting a positive electrode plate or a negative electrode plate with high compacted density; and (4) reducing weights of components of the lithium-ion battery.

Improvements to a current collector are generally selecting a current collector with a light weight or small thickness. For example, a punched current collector or a plastic current collector plated with a metal layer may be used.

For an electrode plate and a battery that use a plastic current collector plated with a metal layer, although energy density is increased, some performance degradations may be caused in terms of machinability, safety performance, electrical performance, and the like. To obtain an electrode plate and a current collector with good electrochemical performance, a plurality of improvements are still needed.

SUMMARY

In view of this, this application provides an electrode plate, an electrochemical apparatus, a battery module, a battery pack, and a device

According to a first aspect, this application provides an electrode plate, including a current collector and an electrode active material layer disposed on at least one surface of the current collector, where the current collector includes a support layer and a conductive layer disposed on at least one surface of the support layer, a single-side thickness D2 of the conductive layer satisfies 30 nm≤D2≤3 μm, and a conductive primer layer including a conductive material and a bonding agent is further disposed between the current collector and the electrode active material layer.

According to a second aspect, this application relates to an electrochemical apparatus, including a positive electrode plate, a negative electrode plate, a separator, and an electrolyte, wherein the positive electrode plate and/or the negative electrode plate are/or the electrode plate in the first aspect of this application.

According to a third aspect, this application relates to a battery module, including the electrochemical apparatus in the second aspect of this application.

According to a fourth aspect, this application relates to a battery pack, including the battery module in the third aspect of this application.

According to a fifth aspect, this application relates to a device, including the electrochemical apparatus in the second aspect of this application, where the electrochemical apparatus is used as a power supply for the device; and the device includes a mobile device, an electric vehicle, an electric train, a satellite, a ship, and an energy storage system.

The conductive primer layer can improve a composite current collector interface, increase a bonding force between the current collector and an active substance, and ensure that the electrode active material layer is more firmly disposed on the surface of the composite current collector. In addition, this can properly overcome disadvantages such as poor conductivity of the composite current collector and vulnerability to damage of the conductive layer of the composite current collector. Because a conductive network between the current collector, the conductive primer layer, and the active substance is effectively repaired and established, electronic transmission efficiency is improved, and resistance between the current collector and the electrode active material layer is reduced. Therefore, direct current resistance in a cell can be effectively reduced, power performance of the cell is improved, and it is ensured that phenomena such as great polarization and lithium precipitation do not easily occur in a long cycling process of the cell, that is, long-term reliability of the cell is effectively improved. Therefore, the electrode plate and electrochemical apparatus in this application have good balanced electrical performance, safety performance, and machinability.

Because the electrochemical apparatus is included, the battery module, battery pack, and device in this application have at least the same advantages as the electrochemical apparatus.

BRIEF DESCRIPTION OF DRAWINGS

The following describes a positive electrode plate, an electrochemical apparatus, and beneficial effects thereof in this application in detail with reference to the accompanying drawings and specific embodiments.

FIG. 1 is a schematic structural diagram of a positive electrode current collector according to a specific embodiment of this application;

FIG. 2 is a schematic structural diagram of a positive electrode current collector according to another specific embodiment of this application;

FIG. 3 is a schematic structural diagram of a positive electrode current collector according to another specific embodiment of this application;

FIG. 4 is a schematic structural diagram of a positive electrode current collector according to another specific embodiment of this application;

FIG. 5 is a schematic structural diagram of a negative electrode current collector according to a specific embodiment of this application;

FIG. 6 is a schematic structural diagram of a negative electrode current collector according to another specific embodiment of this application;

FIG. 7 is a schematic structural diagram of a negative electrode current collector according to another specific embodiment of this application;

FIG. 8 is a schematic structural diagram of a negative electrode current collector according to another specific embodiment of this application;

FIG. 9 is a schematic structural diagram of a positive electrode plate according to a specific embodiment of this application;

FIG. 10 is a schematic structural diagram of a positive electrode plate according to another specific embodiment of this application;

FIG. 11 is a schematic structural diagram of a negative electrode plate according to a specific embodiment of this application;

FIG. 12 is a schematic structural diagram of a negative electrode plate according to another specific embodiment of this application;

FIG. 13 is a microscopic observation diagram of a surface of a positive electrode current collector according to a specific embodiment of this application;

FIG. 14 is a schematic structural diagram of an electrochemical apparatus according to a specific embodiment of this application;

FIG. 15 is a schematic structural diagram of a battery module according to a specific embodiment of this application;

FIG. 16 is a schematic structural diagram of a battery pack according to a specific embodiment of this application;

FIG. 17 is an exploded view of FIG. 16; and

FIG. 18 is a schematic diagram of an implementation of a device using an electrochemical apparatus as a power supply.

In the drawings:

PP. positive electrode plate;

-   -   10. positive electrode current collector;         -   101. positive electrode support layer;         -   102. positive electrode conductive layer;         -   103. positive electrode protection layer;     -   11. conductive primer layer;     -   12. positive electrode active material layer;

NP. negative electrode plate;

-   -   20. negative electrode current collector;         -   201. negative electrode support layer;         -   202. negative electrode conductive layer;         -   203. negative electrode protection layer;     -   21. conductive primer layer;     -   22. negative electrode active material layer;     -   1. battery pack;         -   2. upper case;         -   3. lower case;         -   4. battery module; and             -   5. electrochemical apparatus.

DESCRIPTION OF EMBODIMENTS

The following further describes this application with reference to specific embodiments. It should be understood that these specific embodiments are merely intended to describe this application but not to limit the scope of this application.

A first aspect of this application relates to an electrode plate, including a current collector and an electrode active material layer disposed on at least one surface of the current collector, where the current collector includes a support layer and a conductive layer disposed on at least one surface of the support layer, a single-side thickness D2 of the conductive layer satisfies 30 nm≤D2≤3 μm, and a conductive primer layer including a conductive material and a bonding agent is further disposed between the current collector and the electrode active material layer.

Apparently, the electrode plate may be a positive electrode plate or a negative electrode plate. When the electrode plate is a positive electrode plate, correspondingly, the current collector and the electrode active material layer are respectively a positive electrode current collector and a positive electrode active material layer. When the electrode plate is a negative electrode plate, correspondingly, the current collector and the electrode active material layer are respectively a negative electrode current collector and a negative electrode active material layer.

The current collector used for the electrode plate in the first aspect of this application is a composite current collector, and the composite current collector is formed by at least two materials. Structurally, the current collector includes the support layer and the conductive layer disposed on the at least one surface of the support layer, and the single-side thickness D2 of the conductive layer satisfies 30 nm≤D2≤3 μm. Therefore, the conductive layer in the current collector has a conductive function. The thickness D2 of the conductive layer is far less than a thickness of a common metal current collector such as an Al foil or a Cu foil in the prior art (thicknesses of common Al foil and Cu foil metal current collectors are generally 12 μm and 8 μm). Therefore, mass energy density and volume energy density of an electrochemical apparatus (for example, a lithium battery) using the electrode plate can be increased. In addition, when the composite current collector is used as a positive electrode current collector, safety performance of the positive electrode plate in nail penetration can also be greatly improved.

However, because the conductive layer of the composite current collector is thin, conductivity of the composite current collector is poorer than conductivity of a conventional metal current collector (Al foil or Cu foil), and the conductive layer may be easily damaged in an electrode plate machining process, which further affects electrical performance of the electrochemical apparatus. In addition, in an electrode plate rolling process or the like, the support layer (polymeric material or polymeric composite material) of the composite current collector has greater bounce than a conventional metal current collector. Therefore, a bonding force between the support layer and the conductive layer and a bonding force between the composite current collector and the electrode active material layer both need to be enhanced preferably through interface improvement. In the electrode plate according to this application, the conductive primer layer is additionally disposed between the current collector and the electrode active material layer. Specifically, the conductive primer layer is disposed between a conductive layer of the current collector and the electrode active material layer. Therefore, the conductive primer layer can improve an interface between a composite current collector and the electrode active material layer, increase a bonding force between the current collector and the electrode active material layer, and ensure that the electrode active material layer is more firmly disposed on the surface of the composite current collector. In addition, this can properly overcome disadvantages such as poor conductivity of the composite current collector and vulnerability to damage of the conductive layer of the composite current collector. The conductive primer layer effectively repairs and establishes a conductive network between the current collector, the conductive primer layer, and an active substance to improve electronic transmission efficiency and reduce resistance of the electrode plate including the composite current collector. Therefore, direct current resistance (DCR) in a cell can be effectively reduced, power performance of the cell is improved, and it is ensured that phenomena such as great polarization and lithium precipitation do not easily occur in a long cycling process of the cell, that is, long-term reliability of the cell is effectively improved.

The following describes in detail a structure, material, performance, and the like of the electrode plate (and the current collector in the electrode plate) in an implementation of this application.

[Conductive Layer of the Current Collector]

In comparison with a conventional metal current collector, in the current collector in an implementation of this application, the conductive layer has a conductive function and a current collection function, and is configured to provide electrons for the electrode active material layer.

A material of the conductive layer is selected from at least one of a metal conductive material and a carbon-based conductive material.

The metal conductive material is one selected from at least one of aluminum, copper, nickel, titanium, silver, a nickel-copper alloy, and an aluminum-zirconium alloy.

The carbon-based conductive material is one selected from at least one of graphite, acetylene black, graphene, a carbon nano-tube.

The material of the conductive layer is preferably the metal conductive material, that is, the conductive layer is preferably a metal conductive layer. When the current collector is a positive electrode current collector, aluminum is generally used as the material of the conductive layer. When the current collector is a negative electrode current collector, copper is generally used as the material of the conductive layer.

When conductivity of the conductive layer is poor or the thickness of the conductive layer is excessively small, great resistance and great polarization are caused in the battery. When the thickness of the conductive layer is excessively great, the conductive layer cannot improve mass energy density and volume energy density of the battery.

The single-side thickness of the conductive layer is D2, and D2 preferably satisfies 30 nm≤D2≤3 μm, more preferably, 300 nm≤D2≤2 μm, and most preferably, 500 nm≤D2≤1.5 μm, to better ensure both a light weight and good conductivity of the current collector.

In a preferred implementation of this application, an upper limit of the single-side thickness D2 of the conductive layer may be 3 μm, 2.5 μm, 2 μm, 1.8 μm, 1.5 μm, 1.2 μm, 1 μm, or 900 nm; a lower limit of the single-side thickness D2 of the conductive layer may be 800 nm, 700 nm, 600 nm, 500 nm, 450 nm, 400 nm, 350 nm, 300 nm, 100 nm, 50 nm, or 30 nm. A range of the single-side thickness D2 of the conductive layer may include any numeric value of the upper limit or the lower limit. Preferably, 300 nm≤D2≤2 μm. More preferably, 500 nm≤D2≤1.5 μm.

Because the thickness of the conductive layer in this application is small, damage such as a crack may be easily generated in an electrode plate preparation process or the like. In this case, the conductive primer layer introduced in the electrode plate may buffer and protect the conductive layer, and may form “a repair layer” on a surface of the conductive layer, to improve the bonding force and contact resistance between the current collector and the active material layer.

Generally, a crack exists in the conductive layer of the electrode plate in this application. The crack in the conductive layer generally exists in the conductive layer irregularly. It may be a long strip-shaped crack, or may be a cross-shaped crack, or may be a scattering crack, or may be a crack that penetrates the entire conductive layer, or may be a crack formed on the surface of the conductive layer. The crack in the conductive layer is generally caused by rolling, an excessively great amplitude of a tab during welding, an excessively great tension in substrate wrapping, or the like in the electrode plate machining process.

The conductive layer may be formed on the support layer by using at least one of mechanical rolling, bonding, vapor deposition, and electroless plating. The vapor deposition method is a physical vapor deposition (Physical Vapor Deposition, PVD) method. The vapor deposition method is preferably at least one of an evaporation method and a sputtering method. The evaporation method is one selected from at least one of a vacuum evaporating method, a thermal evaporation method, and an electron beam evaporation method. The sputtering method is preferably a magnetron sputtering method.

At least one of the vapor deposition method or the electroless plating method is preferred, so that binding between the support layer and the conductive layer is firmer.

[Support Layer of the Current Collector]

In the current collector in an implementation of this application, the support layer has functions of supporting and protecting the conductive layer. Because the support layer generally uses an organic polymeric material, density of the support layer is generally less than density of the conductive layer. Therefore, mass energy density of the battery can be significantly increased in comparison with a conventional metal current collector.

Moreover, a metal layer having a small thickness can further increase the mass energy density of the battery. In addition, because the support layer can properly carry and protect the conductive layer located on the surface of the support layer, a common phenomenon of electrode break for conventional current collectors is unlikely to occur.

A material of the support layer is selected from at least one of an insulating polymeric material, an insulating polymeric composite material, a conductive polymeric material, and a conductive polymeric composite material.

For example, the insulating polymeric material is selected from at least one of polyamide, polyterephthalate, polyimide, polyethylene, polypropylene, polystyrene, polyvinyl chloride, aramid fiber, polydiformylphenylenediamine, acrylonitrile-butadiene-styrene copolymer, polybutylene terephthalate, poly-p-phenylene terephthamide, poly(p-phenylene ether), polyoxymethylene, epoxy resin, phenolic resin, polytetrafluoroethylene, p-phenylene sulfide, polyvinylidene fluoride, silicon rubber, polycarbonate, cellulose and a derivative thereof, amylum and a derivative thereof, protein and a derivative thereof, polyvinyl alcohol and a crosslinking agent thereof, and polyethylene glycol and a crosslinking agent thereof.

For example, the insulating polymeric composite material is selected from a composite material formed by an insulating polymeric material and an inorganic material, where the inorganic material is one selected from at least one of a ceramic material, a glass material, and a ceramic composite material.

For example, the conductive polymeric material is selected from a polymeric polysulfur nitride material, or a doped conjugated polymeric material, for example, at least one of polypyrrole, polyacetylene, polyaniline, and polythiophene.

For example, the conductive polymeric composite material is selected from a composite material formed by an insulating polymeric material and a conductive material, where the conductive material is selected from at least one of a conductive carbon material, a metal material, and a composite conductive material, the conductive carbon material is selected from at least one of carbon black, a carbon nano-tube, graphite, acetylene black, and graphene, the metal material is selected from at least one of nickel, iron, copper, aluminum, or an alloy thereof, and the composite conductive material is selected from at least one of nickel-coated graphite powder and nickel-coated carbon fiber.

A person skilled in the art may properly select and determine the material of the support layer based on factors such as actual requirements in an application environment and costs. In this application, the material of the support layer is an insulating polymeric material or an insulating polymeric composite material, especially when the current collector is a positive electrode current collector.

When the current collector is a positive electrode current collector, a special current collector that is supported by an insulating layer and has a specific thickness may be used to apparently improve safety performance of the battery. Because the insulating layer is non-conductive, its resistance is great. Therefore, when a short circuit occurs in the battery in an abnormal case, short circuit resistance can be increased, and a short circuit current can be greatly reduced. Therefore, heat generated in the short circuit can be greatly reduced, and safety performance of the battery can be improved. In addition, because the conductive layer is thin, the conductive network is locally cut off in an abnormal case such as nail penetration, to avoid a short circuit in a large area of the electrochemical apparatus or even in the entire electrochemical apparatus. Therefore, damage caused by nail penetration or the like to the electrochemical apparatus can be limited to a penetration point, and only “a point circuit break” is formed, without affecting normal working of the electrochemical apparatus in a period of time.

A thickness of the support layer is D1, and D1 preferably satisfies 1 μm≤D1≤30 μm, and more preferably, 1 μm≤D1≤15 μm.

If the support layer is excessively thin, mechanical strength of the support layer is insufficient, and the support layer may easily break in the electrode plate machining process or the like. If the support layer is excessively thick, volume energy density of the battery using the current collector is reduced.

An upper limit of the thickness D1 of the support layer may be 30 μm, 25 μm, 20 μm, 15 μm, 12 μm, 10 μm, or 8 μm. A lower limit of the thickness D1 may be 1 μm, 1.5 μm, 2 μm, 3 μm, 4 μm, 5 μm, 6 μm, or 7 μm. A range of the thickness D1 of the support layer may include any numeric value of the upper limit or the lower limit. Preferably, 1 μm≤D1≤15 μm; more preferably, 2 μm≤D1≤10 μm; and most preferably, 3 μm≤D1≤8 μm.

In addition, the specific thickness in this application can further ensure that the current collector has great resistance, and significantly reduce a battery temperature increase when a short circuit occurs in the battery. When the conductive layer is made of aluminum, this can further significantly reduce or prevent a thermite reaction of the positive electrode current collector, and ensure good safety performance of the battery.

In addition, when the conductive layer is a metal conductive layer, a room-temperature Young's modulus of the support layer preferably satisfies 20 Gpa≥E≥4 Gpa.

In this application, a method for testing the room-temperature Young's modulus of the support layer is as follows:

taking a support layer sample, and cutting the sample to 15 mm×200 mm; using a ten-thousandth micrometer to measure a thickness h (μm) of the sample; using a high-speed rail tensile machine to perform a tensile test at a room temperature, setting an initial position, and fixing a length of the sample between jigs to 50 mm; performing stretching at a speed of 50 mm/min, and recording a load L (N) and a device displacement y (mm) when stretching to break, where stress ε=L/(15*h)*1000, and strain η=y/50*100; and drawing a stress-strain curve, and taking a curve in an initial linear area, where a slope of the curve is a Young's modulus E.

Metal is more rigid, that is, less deformed in the electrode plate machining process such as rolling, than a polymeric material or polymeric composite material. Therefore, to ensure that a deformation difference between the support layer and the conductive layer is not excessively great, which may otherwise cause the conductive layer to break, the room-temperature Young's modulus of the support layer preferably satisfies 20 Gpa≥E≥4 Gpa, so that the support layer can have certain rigidity and that matching of rigidity between the support layer and the conductive layer can be further improved. In this way, it is ensured that the deformation difference between the support layer and the conductive layer is not excessively great in a machining process of the current collector and the electrode plate.

Because the support layer has certain rigidity (20 Gpa≥E≥4 Gpa), the current collector is unlikely to deform or extend excessively in the machining process of the current collector and the electrode plate. Therefore, the conductive layer can be firmly bound to the support layer and is unlikely to fall off, and damage of the conductive layer caused by “passive” extension of the conductive layer can be prevented. In addition, the current collector according to this application has certain tenacity, so that the current collector and the electrode plate have certain capabilities to withstand deformation and do not easily break apart.

However, the Young's modulus of the support layer cannot be excessively great; otherwise, there is difficulty in winding, and machinability becomes poor. When 20 Gpa≥E, it can be ensured that the support layer has certain flexibility, and the electrode plate can also have a certain capability to withstand deformation.

In addition, a thermal shrinkage rate of the support layer at 90° C. is preferably not higher than 1.5%. Therefore, thermal stability of the current collector in the electrode plate machining process can be better ensured.

[Protection Layer of the Current Collector]

In some preferred implementations of this application, the current collector is further provided with a protection layer. The protection layer is disposed on one surface of the conductive layer of the current collector or disposed on two surfaces of the conductive layer of the current collector, that is, a surface of the conductive layer away from the support layer and a surface facing the support layer.

The protection layer may be a metal protection layer or a metal oxide protection layer. The protection layer can prevent the conductive layer of the current collector from being broken by chemical corrosion or mechanical damage. In addition, the protection layer can further enhance mechanical strength of the current collector.

Preferably, protection layers are disposed on the two surfaces of the conductive layer of the current collector. A lower protection layer of the conductive layer (that is, a protection layer disposed on the surface of the conductive layer that faces the support layer) can not only prevent the conductive layer from being damaged and enhance mechanical strength of the current collector, but also enhance the bonding force between the support layer and the conductive layer and prevent film detachment (that is, the conductive layer is detached from the support layer).

A technical effect of an upper protection layer of the conductive layer (that is, a protection layer disposed on the surface of the conductive layer away from the support layer) is mainly to prevent the conductive layer from being destructed or corroded or the like in the machining process (for example, the surface of the conductive layer may be affected by immersion in an electrolyte or rolling). In the electrode plate in this application, the conductive primer layer is used to repair a possible crack generated in a process of rolling, winding, or the like, enhance conductivity, and compensate for disadvantages of the composite current collector used as a current collector. Therefore, the upper protection layer of the conductive layer and the conductive primer layer can cooperate to further protect the conductive layer, and jointly improve conducting performance of the composite current collector used as a current collector.

Thanks to good conductivity, the metal protection layer can not only further improve mechanical strength and corrosion resistance of the conductive layer, but also reduce polarization of the electrode plate. For example, a material of the metal protection layer is selected from at least one of nickel, chromium, a nickel-based alloy, and a cooper-based alloy, and is nickel or a nickel-based alloy.

The nickel-based alloy is an alloy formed by adding one or more other elements to a pure nickel matrix, and is preferably a nickel-chromium alloy. The nickel-chromium alloy is an alloy formed by metal nickel and metal chromium. Optionally, a molar ratio of a nickel element to a chromium element is 1:99 to 99:1.

The cooper-based alloy is an alloy formed by adding one or more other elements to a pure cooper matrix, and is preferably a copper-nickel alloy. Optionally, in the copper-nickel alloy, a molar ratio of a nickel element to a copper element is 1:99 to 99:1.

When metal oxide is used for the protection layer, because the metal oxide has low ductility, a large specific surface area, and great hardness, the protection layer can also provide effective support and protection for the conductive layer, and have a good technical effect for improving the bonding force between the support layer and the conductive layer. For example, a material of the metal oxide protection layer is selected from at least one of aluminum oxide, cobalt oxide, chromium oxide, and nickel oxide.

When used as a positive electrode current collector, the composite current collector according to this application preferably uses metal oxide as its protection layer to further improve safety performance of the positive electrode plate and battery while achieving a good technical effect of support and protection. When used as a negative electrode current collector, the composite current collector according to this application preferably uses metal as its protection layer to further improve conductivity of the electrode plate and kinetic performance of the battery to further reduce polarization of the battery, while achieving a good technical effect of support and protection.

A thickness of the protection layer is D3, and D3 preferably satisfies D3≤ 1/10 D2, and 1 nm≤D3≤200 nm. If the protection layer is excessively thin, the conductive layer cannot be protected sufficiently. If the protection layer is excessively thick, mass energy density and volume energy density of the battery may be reduced. Preferably, 5 nm≤D3≤500 nm; more preferably, 10 nm≤D3≤200 nm; and most preferably, 10 nm≤D3≤50 nm.

Materials of the protection layers located on the two surfaces of the conductive layer may be the same or different, and thicknesses thereof may be the same or different.

Preferably, a thickness of the lower protection layer is less than a thickness of the upper protection layer. This helps improve mass energy density of the battery.

Further optionally, a proportional relationship between a thickness D3″ of the lower protection layer and a thickness D3′ of the upper protection layer is: ½ D3′≤D3″≤⅘ D3′.

When the current collector is a positive electrode current collector, aluminum is generally used as the material of the conductive layer, and a metal oxide material is preferably used as a material of the lower protection layer. In comparison with metal used as the material of the lower protection layer, the metal oxide material has greater resistance. Therefore, this type of lower protection layer can further increase resistance of the positive electrode current collector to some extent, further increase short circuit resistance when a short circuit occurs in the battery in an abnormal case, and improve safety performance of the battery. In addition, because a specific surface area of the metal oxide is larger, a bonding force between the lower protection layer made of the metal oxide material and the support layer is enhanced. In addition, because the specific surface area of the metal oxide is larger, the lower protection layer can increase roughness of the surface of the support layer, enhance the bonding force between the conductive layer and the support layer, and increase overall strength of the current collector.

When the current collector is a negative electrode current collector, cooper is generally used as the material of the conductive layer, and a metal material is preferably used as the material of the protection layer. More preferably, on a basis of including at least one metal protection layer, at least one of the upper protection layer and the lower protection layer further includes a metal oxide protection layer, to improve both conductivity and an interface bonding force of the negative electrode composite current collector.

[Current Collector]

FIG. 1 to FIG. 8 show schematic structural diagrams of current collectors used in electrode plates in some implementations of this application.

Schematic diagrams of positive electrode current collectors are shown in FIG. 1 to FIG. 4.

In FIG. 1, a positive electrode current collector 10 includes a positive electrode support layer 101 and positive electrode current collector conductive layers 102 that are disposed on two opposite surfaces of the positive electrode current collector support layer 101, and further includes positive electrode current collector protection layers 103, that is, lower protection layers, disposed on lower surfaces of the positive electrode current collector conductive layers 102 (that is, surfaces facing the positive electrode current collector support layer 101).

In FIG. 2, a positive electrode current collector 10 includes a positive electrode current collector support layer 101 and positive electrode current collector conductive layers 102 that are disposed on two opposite surfaces of the positive electrode current collector support layer 101, and further includes positive electrode current collector protection layers 103, that is, lower protection layers and upper protection layers, disposed on two opposite surfaces of the positive electrode current collector conductive layers 102.

In FIG. 3, a positive electrode current collector 10 includes a positive electrode current collector support layer 101 and a positive electrode current collector conductive layer 102 disposed on one surface of the positive electrode current collector support layer 101, and further includes a positive electrode current collector protection layer 103, that is, a lower protection layer, disposed on a surface of the positive electrode current collector conductive layer 102 that faces the positive electrode current collector support layer 101.

In FIG. 4, a positive electrode current collector 10 includes a positive electrode current collector support layer 101 and a positive electrode current collector conductive layer 102 disposed on one surface of the positive electrode current collector support layer 101, and further includes positive electrode current collector protection layers 103, that is, a lower protection layer and an upper protection layer, disposed on two opposite surfaces of the positive electrode current collector conductive layer 102.

Likewise, schematic diagrams of negative electrode current collectors are shown in FIG. 5 to FIG. 8.

In FIG. 5, a negative electrode current collector 20 includes a negative electrode current collector support layer 201 and negative electrode current collector conductive layers 202 that are disposed on two opposite surfaces of the negative electrode current collector support layer 201, and further includes negative electrode current collector protection layers 203, that is, lower protection layers, disposed on surfaces of the negative electrode current collector conductive layers 202 that face the negative electrode current collector support layer 201.

In FIG. 6, a negative electrode current collector 20 includes a negative electrode current collector support layer 201 and negative electrode current collector conductive layers 202 that are disposed on two opposite surfaces of the negative electrode current collector support layer 201, and further includes negative electrode current collector protection layers 203, that is, lower protection layers and upper protection layers, disposed on two opposite surfaces of the negative electrode current collector conductive layers 202.

In FIG. 7, a negative electrode current collector 20 includes a negative electrode current collector support layer 201 and a negative electrode current collector conductive layer 202 disposed on one surface of the negative electrode current collector support layer 201, and further includes a negative electrode current collector protection layer 203, that is, a lower protection layer, disposed on the negative electrode current collector conductive layer 202 in face of the negative electrode current collector support layer 201.

In FIG. 8, a negative electrode current collector 20 includes a negative electrode current collector support layer 201 and a negative electrode current collector conductive layer 202 disposed on one surface of the negative electrode current collector support layer 201, and further includes negative electrode current collector protection layers 203, that is, a lower protection layer and an upper protection layer, disposed on two opposite surfaces of the negative electrode current collector conductive layer 202.

Materials of the protection layers located on the two opposite surfaces of the conductive layer may be the same or different, and thicknesses thereof may be the same or different.

For the current collector used for the electrode plate according to this application, conductive layers may be disposed on two opposite surfaces of the support layer, as shown in FIG. 1, FIG. 2, FIG. 5, and FIG. 6; or a conductive layer may be disposed on only one surface of the support layer, as shown in FIG. 3, FIG. 4, FIG. 7, and FIG. 8.

In addition, although the composite current collector used for the electrode plate in this application preferably includes the protection layer of the current collector as shown in FIG. 1 to FIG. 8, it should be understood that the protection layer of the current collector is not a necessary structure of the current collector. In some implementations, the used current collector may not include the protection layer of the current collector.

[Conductive Primer Layer of the Electrode Plate]

The conductive primer layer includes the conductive material and the bonding agent.

Based on a total weight of the conductive primer layer, a weight percentage of the conductive material is 10% to 99%, preferably, 20% to 80%, and more preferably 50% to 80%; and a weight percentage of the bonding agent is 1% to 90%, preferably, 20% to 80%, and more preferably 20% to 50%. These percentages can help improve conductivity of the electrode plate and a bonding force between the current collector and the electrode active material layer.

The conductive material is at least one of a conductive carbon material and a metal material.

The conductive carbon material is selected from at least one of zero-dimensional conductive carbon (such as acetylene black or conductive carbon black), one-dimensional conductive carbon (such as a carbon nano-tube), two-dimensional conductive carbon (such as conductive graphite or graphene), and three-dimensional conductive carbon (such as reduced graphene oxide), and the metal material is selected from at least one of aluminum powder, iron powder, and silver powder.

The conductive material preferably includes a two-dimensional conductive carbon material. After the two-dimensional conductive carbon material is added, in a plate compaction process, the two-dimensional conductive carbon material in the conductive primer layer may implement a buffer function, reduce damage to the conductive layer of the current collector in a compaction process, and reduce a crack by generating “horizontal sliding”. A particle diameter D50 of the two-dimensional conductive carbon material is preferably 0.01 μm to 0.1 μm. The two-dimensional conductive carbon material preferably accounts for 1 wt % to 50 wt % of the conductive material.

The bonding agent is selected from at least one of styrene butadiene rubber, oil-based polyvinylidene fluoride (PVDF), polyvinylidene fluoride copolymer (for example, PVDF-HFP copolymer or PVDF-TFE copolymer), sodium carboxymethyl cellulose, polystyrene, polyacrylic acid, polytetrafluoroethylene, polyacrylonitrile, polyimide, water-based PVDF, polyurethane, polyvinyl alcohol, polyacrylate, polyacrylic-acid-polyacrylonitrile copolymer, and polyacrylate-polyacrylonitrile copolymer.

The bonding agent is preferably a water-based bonding agent, for example, at least one of water-based PVDF, polyacrylic acid, polyurethane, polyvinyl alcohol, polyacrylate, polyacrylic-acid-polyacrylonitrile copolymer, and polyacrylate-polyacrylonitrile copolymer. Therefore, DCR of the electrochemical apparatus does not increase significantly. In this application, a “water-based” polymeric material means that a molecular chain of a polymer completely extends and dissolves in water; and an “oil-based” polymeric material means that a molecular chain of a polymer completely extends and dissolves in an oil-based solvent. A person skilled in the art understands that an appropriate surfactant may be used to dissolve a same type of polymeric material into water and oil separately, that is, a same type of polymeric material may be made into a water-based polymeric material and an oil-based polymeric material separately by using an appropriate surfactant. For example, a person skilled in the art may change PVDF into water-based PVDF or oil-based PVDF based on a requirement.

A single-side thickness H of the conductive primer layer is 0.1 μm to 5 μm; and preferably, a ratio of H to D2 is 0.5:1 to 5:1. If the ratio of H/D2 is excessively low, the crack of the conductive layer cannot be effectively improved, and conductivity of the electrode plate cannot be effectively improved. If the ratio is excessively high, not only mass energy density of the battery is reduced, but also DCR of the battery is increased, and this is disadvantageous for improving kinetic performance of the battery.

[Electrode Active Material Layer of the Electrode Plate]

The electrode active material layer used for the electrode plate in this application may be various conventional common electrode active material layers in the art, and its composition and preparation method are commonly known in the art. The electrode active material layer generally includes an electrode active material, a bonding agent, and a conductive agent. Based on a requirement, the electrode active material layer may further include other optional additives or auxiliaries.

For the electrode plate in this application, an average particle diameter D50 of the active material in the electrode active material layer is preferably 5 μm to 15 μm. If D50 is excessively small, after compaction, a porosity of the electrode plate is small and disadvantageous for infiltration of an electrolyte, and a large specific surface area of the electrode plate is likely to produce a plurality of side reactions with the electrolyte, hence reducing reliability of the cell. If D50 is excessively large, great damage may be easily caused to the conductive primer layer and the composite current collector in an electrode plate compaction process. D50 is a corresponding particle diameter when a cumulative volume percentage of the active material reaches 50%, that is, a median particle diameter in volume distribution. For example, D50 may be measured by using a laser diffraction particle diameter distribution measuring instrument (for example, Malvern Mastersizer 3000).

Moreover, for the electrode plate in this application, when content of the bonding agent in the electrode active material layer is generally high, there is a strong bonding force between the active material layer and the conductive primer layer, so that there is also a strong bonding force between an entire membrane layer (that is, a collective term of the active material layer and the conductive primer layer) and the composite current collector, and in an abnormal case such as nail penetration, the active material layer (or the membrane layer) can effectively wrap metal burrs generated in the conductive layer, to improve safety performance of the battery in nail penetration. Therefore, for further safety improvement of the battery, preferably, based on a total weight of the electrode active material layer, the content of the bonding agent in the positive electrode active material layer is not less than 1 wt %, and preferably, not less than 1.5 wt %. When the content of the bonding agent is kept at a specific value, there is a strong bonding force between the active material layer and the conductive primer layer, so that in an abnormal case such as nail penetration, the active material layer can effectively wrap metal burrs generated in the conductive layer, to improve safety performance of the battery in nail penetration.

For a positive electrode plate, various common electrode active materials in the art (that is, positive electrode active materials) may be used. For example, for the lithium battery, a positive electrode active material may be selected from lithium cobalt oxide, lithium nickel oxide, lithium manganese oxide, lithium nickel manganese oxide, lithium nickel cobalt manganese oxide, lithium nickel cobalt aluminum oxide, transition metal phosphate, lithium iron phosphate, and the like. However, this application is not limited to these materials, and may further use other conventional well-known materials that can be used as positive electrode substances of the lithium-ion battery. One of these positive electrode active materials may be used alone, or two or more may be used in combination. Preferably, the positive electrode active material may be selected from one or more of LiCoO2, LiNiO2, LiMnO2, LiMn2O4, LiNi1/3Co1/3Mn1/3O2 (NCM333), LiNi0.5Co0.2Mn0.3O2 (NCM523), LiNi0.6Co0.2Mn0.2O2 (NCM622), LiNi0.8Co0.1Mn0.1O2 (NCM811), LiNi0.85Co0.15Al0.05O2, LiFePO4, and LiMnPO4.

For a negative electrode plate, various common electrode active materials in the art (that is, negative electrode active materials) may be used. For example, for the lithium battery, a negative electrode active material may be selected from carbon materials such as graphite (artificial graphite or natural graphite), conductive carbon black, and carbon fiber, metal or semimetal materials or alloys thereof such as Si, Sn, Ge, Bi, Sn, and In, lithium nitride or lithium oxide, lithium metal or a lithium alloy, and the like.

It is well known to a person skilled in the art that the electrode active material layer can be obtained by performing post-processing such as drying on a slurry including the electrode active material, the conductive agent, the bonding agent, and the like that is coated onto the electrode current collector (or pre-coated onto the primer layer of the electrode current collector).

[Electrode Plate]

FIG. 9 to FIG. 12 show schematic structural diagrams of electrode plates in some implementations of this application.

Schematic diagrams of positive electrode plates are shown in FIG. 9 and FIG. 10.

In FIG. 9, a positive electrode plate PP includes a positive electrode current collector 10, and conductive primer layers 11 and positive electrode active material layers 12 that are disposed on two opposite surfaces of the positive electrode current collector 10, where the positive electrode current collector 10 includes a positive electrode current collector support layer 101, and positive electrode current collector conductive layers 102 that are disposed on two opposite surfaces of the positive electrode current collector support layer 101.

In FIG. 10, a positive electrode plate PP includes a positive electrode current collector 10, and a conductive primer layer 11 and a positive electrode active material layer 12 that are disposed on one surface of the positive electrode current collector 10, where the positive electrode current collector 10 includes a positive electrode current collector support layer 101, and a positive electrode current collector conductive layer 102 that is disposed on one surface of the positive electrode current collector support layer 101.

Schematic diagrams of negative electrode plates are shown in FIG. 11 and FIG. 12.

In FIG. 11, a negative electrode plate NP includes a negative electrode current collector 20, and conductive primer layers 21 and negative electrode active material layers 22 that are disposed on two opposite surfaces of the negative electrode current collector 20, where the negative electrode current collector 20 includes a negative electrode current collector support layer 201, and negative electrode current collector conductive layers 202 that are disposed on two opposite surfaces of the negative electrode current collector support layer 201.

In FIG. 12, a negative electrode plate NP includes a negative electrode current collector 20, and conductive primer layers 21 and a negative electrode active material layer 22 that are disposed on one surface of the negative electrode current collector 20, where the negative electrode current collector 20 includes a negative electrode current collector support layer 201, and a negative electrode current collector conductive layer 202 that is disposed on one surface of the negative electrode current collector support layer 201.

As shown in FIG. 9 to FIG. 12, an electrode active material layer may be disposed on one surface of a current collector, or may be disposed on two surfaces of a current collector.

A person skilled in the art may understand that when a current collector provided with conductive layers on both sides is used, both sides of an electrode plate may be coated (that is, electrode active material layers are disposed on two surfaces of the current collector), or a single side of the electrode plate may be coated (that is, an electrode active material layer is disposed on only one surface of the current collector); when a current collector provided with a conductive layer only on a single side is used, only a single side of an electrode plate can be coated, and only the side of the current collector on which the conductive layer is disposed can be coated with an electrode active material layer (and a conductive primer layer).

[Electrochemical Apparatus]

A second aspect of this application relates to an electrochemical apparatus, including a positive electrode plate, a negative electrode plate, a separator, and an electrolyte, where the positive electrode plate and/or the negative electrode plate are/or the electrode plate according to the first aspect of this application.

The electrochemical apparatus may be a capacitor, a primary battery, or a secondary battery. For example, the electrochemical apparatus may be a lithium-ion capacitor, a lithium-ion primary battery, or a lithium-ion secondary battery. A method for constructing and preparing the electrochemical apparatus is well known, except that a positive electrode plate and/or a negative electrode plate in this application are/is used. Because the electrode plate in this application is used, the electrochemical apparatus has improved safety (for example, safety in nail penetration) and electrical performance. In addition, because the electrode plate in this application can be easily machined, manufacturing costs of the electrochemical apparatus using the electrode plate in this application can be reduced.

In the electrochemical apparatus in this application, specific types and composition of the separator and the electrolyte are not specifically limited, and may be selected based on an actual requirement. Specifically, the separator may be selected from a polyethylene film, a polypropylene film, a polyvinylidene fluoride film, and a multi-layer composite film thereof. When the battery is a lithium-ion battery, a non-aqueous electrolyte is generally used as its electrolyte. As a non-aqueous electrolyte, a lithium salt solution dissolved in an organic solvent is generally used. For example, lithium salt is inorganic lithium salt such as LiClO4, LiPF6, LiBF4, LiAsF6, or LiSbF6, or organic lithium salt such as LiCF3SO3, LiCF3CO2, Li2C2F4 (SO3)2, LiN (CF3SO2)2, LiC (CF3SO2)3, or LiCnF2n+1SO3 (n≥2). For example, the organic solvent used for the non-aqueous electrolyte is cyclic carbonate such as ethylene carbonate, propylene carbonate, butylene carbonate, or vinylene carbonate, or chain carbonate such as dimethyl carbonate, diethyl carbonate, or ethyl methyl carbonate, or chain ester such as methyl propionate, or cyclic ester such as γ-butyrolactone, or chain ether such as dimethoxyethane, diethyl ether, diethylene glycol dimethyl ether, or triethylene glycol dimethyl ether, or cyclic ether such as tetrahydrofuran or 2-methyltetrahydrofuran, or nitrile such as acetonitrile or propionitrile, or a mixture of these solvents.

[Battery Module]

A third aspect of this application relates to a battery module, including any electrochemical apparatus or several electrochemical apparatuses in the second aspect of this application.

Further, a quantity of electrochemical apparatuses included in the battery module may be adjusted based on an application and a capacity of the battery module.

In some embodiments, referring to FIG. 14 and FIG. 15, a plurality of electrochemical apparatuses 5 in a battery module 4 are arranged in sequence along a length direction of the battery module 4. Certainly, an arrangement may be made in any other manner. Further, the plurality of electrochemical apparatuses 5 may be fixed by using fasteners. Optionally, the battery module 4 may further include a housing that has an accommodating space, and the plurality of electrochemical apparatuses 5 are accommodated in the accommodating space.

[Battery Pack]

A fourth aspect of this application relates to a battery pack, including any battery module or several battery modules in the third aspect of this application. To be specific, the battery pack includes any electrochemical apparatus or several electrochemical apparatuses in the second aspect of this application.

A quantity of battery modules in the battery pack may be adjusted based on an application and a capacity of the battery pack.

In some embodiments, referring to FIG. 16 and FIG. 17, a battery pack 1 may include a battery box and a plurality of battery modules 4 disposed in the battery box. The battery box includes an upper case 2 and a lower case 3. The upper case 2 can cover the lower case 3 to form a closed space for accommodating the battery modules 4. The plurality of battery modules 4 may be arranged in the battery box in any manner.

[Device]

A fifth aspect of this application relates to a device, including any electrochemical apparatus or several electrochemical apparatuses in the second aspect of this application. The electrochemical apparatus may be used as a power supply for the device.

Preferably, the device may be, but is not limited to, a mobile device (for example, a mobile phone or a notebook computer), an electric vehicle (for example, a full electric vehicle, a hybrid electric vehicle, a plug-in hybrid electric vehicle, an electric bicycle, an electric scooter, an electric golf vehicle, or an electric truck), an electric train, a ship, a satellite, an energy storage system, or the like.

For example, FIG. 18 shows a device including an electrochemical apparatus in this application. The device is a full electric vehicle, a hybrid electric vehicle, a plug-in hybrid electric vehicle, or the like, and the electrochemical apparatus in this application supplies power to the device.

Because the electrochemical apparatus provided in this application is included, the battery module, battery pack, and device have at least the same advantages as the electrochemical apparatus. Details are not described again herein.

A person skilled in the art may understand that the foregoing definitions or preferred ranges of component selection, component content, and material physicochemical performance parameters of the conductive primer layer, the electrode active material layer, and the like in different implementations of this application may be randomly combined, and various implementations obtained through the combination shall still fall within the scope of this application and shall be considered as a part of content disclosed in this specification.

Unless otherwise specified, various parameters in this specification have general meanings well known in the art, and may be measured by using a method well known in the art. For example, a test may be performed according to a method provided in an embodiment of this application. In addition, preferred ranges and options of different parameters provided in various preferred implementations may be randomly combined, and it is considered that various combinations obtained thereby shall fall within the scope of this application.

The following further describes beneficial effects of this application with reference to embodiments.

Embodiments

1. Preparing a Current Collector that does not have a Protection Layer:

A support layer with a certain thickness is selected, and a conductive layer with a certain thickness is formed on a surface of the support layer by vacuum evaporating, mechanical rolling, or bonding.

(1) A formation condition for vacuum evaporating is as follows: A support layer that undergoes surface cleaning processing is placed in a vacuum plating chamber; a high-purity metal wire in a metal evaporating chamber is melted and evaporated at a high temperature of 1600° C. to 2000° C.; and the evaporated metal passes through a cooling system in the vacuum plating chamber and is finally deposited on a surface of the support layer to form a conductive layer.

(2) A formation condition for mechanical rolling is as follows: A foil of a conductive layer material is placed in a mechanical roller; a pressure of 20t to 40t is applied to the foil to roll the foil to a predetermined thickness; then the foil is placed on a surface of a support layer that undergoes surface cleaning processing; and finally, the two are placed in the mechanical roller, and a pressure of 30t to 50t is applied, so that the two are tightly bound.

(3) A formation condition for bonding: A foil of a conductive layer material is placed in a mechanical roller; a pressure of 20t to 40t is applied to the foil to roll the foil to a predetermined thickness; then a surface of a support layer that undergoes surface cleaning processing is coated with a mixed solution of PVDF and NMP; and finally, a conductive layer with the predetermined thickness is bonded to the surface of the support layer and dried at 100° C.

2. Preparing a Current Collector that has a Protection Layer:

A current collector that has a protection layer is prepared in the following manners:

(1) First, a protection layer is disposed on a surface of a support layer by using a vapor deposition method or a coating method; then a conductive layer with a certain thickness is formed by vacuum evaporating, mechanical rolling, or bonding, on the surface of the support layer having the protection layer, to prepare a current collector that has a protection layer (the protection layer is located between the support layer and the conductive layer); in addition, on the foregoing basis, another protection layer may be formed on a surface of the conductive layer in a direction away from the support layer by using the vapor deposition method, an in-situ formation method, or the coating method, to prepare the current collector with protection layers (the protection layers are located on two opposite surfaces of the conductive layer).

(2) First, a protection layer is formed on a surface of a conductive layer by using a vapor deposition method, an in-situ formation method, or a coating method; then the conductive layer having the protection layer is disposed on a surface of a support layer by mechanical rolling or bonding, and the protection layer is disposed between the support layer and the conductive layer, to prepare a current collector having a protection layer (the protection layer is located between the support layer and the conductive layer); in addition, on the foregoing basis, another protection layer may be formed on a surface of the conductive layer in a direction away from the support layer by using the vapor deposition method, the in-situ formation method, or the coating method, to prepare the current collector with protection layers (the protection layers are located on two opposite surfaces of the conductive layer).

(3) First, a protection layer is formed on a surface of a conductive layer by using a vapor deposition method, an in-situ formation method, or a coating method; then the conductive layer having the protection layer is disposed on a surface of a support layer by mechanical rolling or bonding, and the protection layer is disposed on the surface of the conductive layer away from the support layer, to prepare a current collector having a protection layer (the protection layer is located on the surface of the conductive layer away from the support layer).

(4) First, protection layers are formed on two surfaces of a conductive layer by using a vapor deposition method, an in-situ formation method, or a coating method; and then the conductive layer having the protection layers is disposed on a surface of a support layer by mechanical rolling or bonding, to prepare a current collector having protection layers (the protection layers are located on two opposite surfaces of the conductive layer).

(5) On a basis of “preparing a current collector that does not have a protection layer” above, a protection layer is formed on a surface of a conductive layer in a direction away from a support layer by using a vapor deposition method, an in-situ formation method, or a coating method, to prepare a current collector having a protection layer (the protection layer is located on the surface of the conductive layer away from the support layer).

In a preparation example, the vapor deposition method uses vacuum evaporating, the in-situ formation method uses in-situ passivating, and the coating method uses blade coating.

A formation condition for vacuum evaporating is as follows: A sample that undergoes surface cleaning processing is placed in a vacuum plating chamber; a protection layer material in an evaporating chamber is melted and evaporated at a high temperature of 1600° C. to 2000° C.; and the evaporated protection layer material passes through a cooling system in the vacuum plating chamber and is finally deposited on a surface of the sample to form a protection layer.

A formation condition for in-situ passivating is as follows: A conductive layer is placed in a high-temperature oxidizing environment, where a temperature is controlled to be 160° C. to 250° C., oxygen supplying in the high-temperature environment is maintained, and processing time is 30 min, so that a metal oxide protection layer is formed.

A formation condition for gravure coating is as follows: A protection layer material and NMP are stirred and mixed; then a sample surface is coated with a slurry of the protection layer material (solid content is 20% to 75%); then a thickness of the coating is controlled by using a gravure roller; and finally, the coating is dried at a temperature of 100° C. to 130° C.

3. Preparing an Electrode Plate:

(1) Positive Electrode Plate in an Embodiment:

A conductive material (such as conductive carbon black) and a bonding agent (such as PVDF or polyacrylic acid) that are proportioned are dissolved in an appropriate solvent (for example, NMP or water), and stirred evenly to prepare a primer slurry.

Two surfaces of a composite current collector prepared according to the foregoing method are evenly coated with the primer slurry at a coating speed of 20 m/min, and a primer layer is dried, where an oven temperature is 70° C. to 100° C., and drying time is 5 min.

After the primer layer is completely dried, 92 wt % positive electrode active material, 5 wt % conductive agent Super-P (“SP” for short), and 3 wt % PVDF are dissolved in an NMP solvent, and evenly stirred to prepare a slurry of the positive electrode active material layer; a surface of the primer layer is coated with the slurry of the positive electrode active material layer by extrusion coating; and after the coating is dried at 85° C., a positive electrode active material layer is obtained.

Then the current collector having various coating layers is cold-pressed and cut, and dried for four hours under an 85° C. vacuum condition, and a tab is welded, so that a positive electrode plate is obtained.

(2) Comparative Positive Electrode Plate:

It is prepared by using a method similar to the method for preparing a positive electrode plate in the foregoing embodiment. However, a slurry of the positive electrode active material layer is directly applied to a surface of a composite current collector, and no primer layer is disposed.

(3) Conventional Positive Electrode Plate:

A current collector is an Al foil with a thickness of 12 μm. By using a method similar to the foregoing method for preparing a comparative positive electrode plate, a slurry of the positive electrode active material layer is directly applied to a surface of the Al foil current collector, and after processing, a conventional positive electrode plate is obtained.

(4) Negative Electrode Plate in an Embodiment:

A conductive material (such as conductive carbon black) and a bonding agent (such as PVDF or polyacrylic acid) that are proportioned are dissolved in an appropriate solvent (for example, NMP or water), and stirred evenly to prepare a primer slurry.

Two surfaces of a composite current collector prepared according to the foregoing method are evenly coated with the primer slurry at a coating speed of 20 m/min, and a primer layer is dried, where an oven temperature is 70° C. to 100° C., and drying time is 5 min.

After the primer layer is completely dried, a negative electrode active substance artificial graphite, a conductive agent Super-P, a thickening agent CMC, and a bonding agent SBR are added based on a mass ratio of 96.5:1.0:1.0:1.5 to a deionized water solvent, and mixed evenly to prepare a slurry of the negative electrode active material layer; a surface of the primer layer is coated with the slurry of the negative electrode active material layer by extrusion coating; and after the coating is dried at 85° C., a negative electrode active material layer is obtained.

Then the current collector having various coating layers is cold-pressed and cut, and dried for four hours under a 110° C. vacuum condition, and a tab is welded, so that a negative electrode plate is obtained.

(5) Comparative Negative Electrode Plate:

It is prepared by using a method similar to the method for preparing a negative electrode plate in the foregoing embodiment. However, a slurry of the negative electrode active material layer is directly applied to a surface of a composite current collector, and no primer layer is disposed.

(6) Conventional Negative Electrode Plate:

A current collector is a Cu foil with a thickness of 8 μm. By using a method similar to the foregoing method for preparing a comparative negative electrode plate, a slurry of the negative electrode active material layer is directly applied to a surface of the Cu foil current collector, and after processing, a conventional negative electrode plate is obtained.

4. Preparing a Battery:

Through a conventional battery preparation process, a positive electrode plate (compacted density: 3.4 g/cm3), a PP/PE/PP separator, and a negative electrode plate (compacted density: 1.6 g/cm3) are wound together into a bare cell, and then placed in a battery housing; an electrolyte (EC-EMC volume ratio: 3:7; LiPF6: 1 mol/L) is injected; then after processes such as sealing and formation, a lithium-ion secondary battery (hereinafter referred to as the battery for short) is finally obtained.

5. Battery Testing Method:

(1) Method for Testing Cycle Life of a Lithium-Ion Battery:

The lithium-ion battery is charged and discharged at 45° C., that is, first charged to 4.2 V by using a 1C current, and then discharged to 2.8 V by using a 1C current, and a discharge capacity in a first cycle is recorded; then the battery is charged and discharged for 1000 cycles by using 1C/1C currents, and a discharge capacity in the 1000th cycle is recorded; the discharge capacity in the 1000th cycle is divided by the discharge capacity in the first cycle, and a capacity retention rate in the 1000th cycle is obtained.

(2) Method for Testing a DCR Growth Rate:

At 25° C., a secondary battery is adjusted to 50% SOC by using a 1C current, and a voltage U1 is recorded. Then the battery is discharged for 30 s by using a 4C current, and a voltage U2 is recorded. DCR=(U1−U2)/4C. Then the battery is charged and discharged for 500 cycles by using 1C/1C currents, and DCR in the 500th cycle is recorded. The DCR in the 500th cycle is divided by the DCR in the first cycle, then 1 is subtracted, and a DCR growth rate in the 500th cycle is obtained.

(3) Pin Penetration Test:

A secondary battery (10 samples) is fully charged to a charging cut-off voltage by using a 1C current, and then constant-voltage charging is performed until the current is reduced to 0.05C. Then charging is stopped. The battery is penetrated at a speed of 25 mm/s in a direction vertical to a battery plate by using a φ8 mm heat-resistant steel pin, where a penetration position is preferably close to a geometric center in a penetrated surface, and the steel pin stays in the battery. Whether a phenomenon of battery burning or explosion occurs is observed.

6. Test Result and Discussion:

6.1. Function of a Composite Current Collector in Improving Mass Energy Density of a Battery

Specific parameters of electrode plates and current collectors thereof in various embodiments are shown in Table 1 (no protection layer is disposed in the current collectors in the embodiments that are listed in Table 1). In Table 1, for a positive electrode current collector, a weight percentage of the current collector is the percentage of a weight of the positive electrode current collector in a unit area in a weight of a conventional positive electrode current collector in a unit area; and for a negative electrode current collector, a weight percentage of the current collector is the percentage of a weight of the negative electrode current collector in a unit area in a weight of a conventional negative electrode current collector in a unit area.

TABLE 1 Weight Thickness percentage of the of the Electrode plate Current collector Support layer Conductive layer current current No. No. Material D1 Material D2 collector collector Positive Positive electrode PI 6 μm Al 300 nm 6.6 μm 30.0% electrode plate 1 current collector 1 Positive Positive electrode PET 4 μm Al 500 nm 5 μm 24.3% electrode plate 2 current collector 2 Positive Positive electrode PET 2 μm Al 200 nm 2.4 μm 11.3% electrode plate 3 current collector 3 Conventional Conventional / / Al / 12 μm  100% positive positive electrode electrode plate current collector Negative Negative electrode PET 5 μm Cu 500 nm 6 μm 21.6% electrode plate 1 current collector 1 Negative Negative electrode PI 2 μm Cu 800 nm 3.6 μm 23.8% electrode plate 2 current collector 2 Negative Negative electrode PET 8 μm Cu 1 μm 10 μm 39.6% electrode plate 3 current collector 3 Negative Negative electrode PET 6 μm Cu 1.5 μm 9 μm 48.5% electrode plate 4 current collector 4 Negative Negative electrode PET 4 μm Cu 1.2 μm 6.4 μm 37.3% electrode plate 5 current collector 5 Negative Negative electrode PET 10 μm  Cu 200 nm 10.4 μm 23.3% electrode plate 6 current collector 6 Negative Negative electrode PI 8 μm Cu 2 μm 12 μm 65.3% electrode plate 7 current collector 7 Conventional Conventional / / Cu / 8 μm  100% negative negative electrode electrode plate current collector

Based on Table 1, it can be known that weights of both a positive electrode current collector and a negative electrode current collector in this application are reduced to different extents in comparison with a conventional current collector, so that mass energy density of a battery can be increased. However, for a current collector, and in particular, for a negative electrode current collector, when a thickness of a conductive layer is greater than 1.5 μm, an extent of weight reduction improved is reduced.

6.2. Function of a Protection Layer in Improving Electrochemical Performance of a Composite Current Collector

On a basis of the current collectors in the embodiments that are listed in Table 1, protection layers are further formed, to facilitate research on functions of the protection layers in improving electrochemical performance of composite current collectors. “Positive electrode current collector 2-1” in Table 2 represents a current collector whose protection layers are formed based on “positive electrode current collector 2” in Table 1. Meanings of numbers of other current collectors are similar to this.

TABLE 2 Upper protection layer Lower protection layer Electrode plate No. Current collector No. Material D3′ Material D3″ Positive electrode Positive electrode Nickel oxide 10 nm Nickel oxide 8 nm plate 2-1 current collector 2-1 Positive electrode Positive electrode Nickel oxide 50 nm Nickel oxide 30 nm plate 2-2 current collector 2-2 Negative electrode Negative electrode / / Nickel 200 nm plate 4-1 current collector 4-1 Negative electrode Negative electrode Nickel 5 nm / / plate 4-2 current collector 4-2 Negative electrode Negative electrode Nickel-based alloy 100 nm / / plate 4-3 current collector 4-3 Negative electrode Negative electrode Nickel 10 nm Nickel 10 nm plate 4-4 current collector 4-4 Negative electrode Negative electrode Nickel 50 nm Nickel 50 nm plate 4-5 current collector 4-5 Negative electrode Negative electrode Nickel 100 nm Nickel 50 nm plate 4-6 current collector 4-6

Table 3 shows cycle performance data obtained through measurement after the electrode plates listed in Table 2 are assembled into batteries.

TABLE 3 Capacity retention rate in a Battery 1000^(th) cycle No. Electrode plate at 45° C. Battery 1 Conventional negative Conventional positive 86.5% electrode plate electrode plate Battery 2 Conventional negative Positive electrode 80.7% electrode plate plate 2 Battery 3 Conventional negative Positive electrode 85.2% electrode plate plate 2-1 Battery 4 Conventional negative Positive electrode 85.4% electrode plate plate 2-2 Battery 5 Negative electrode Conventional positive 86.3% plate 4 electrode plate Battery 6 Negative electrode Conventional positive 87.1% plate 4-1 electrode plate Battery 7 Negative electrode Conventional positive 86.5% plate 4-2 electrode plate Battery 8 Negative electrode Conventional positive 86.7% plate 4-3 electrode plate Battery 9 Negative electrode Conventional positive 87.6% plate 4-4 electrode plate Battery 10 Negative electrode Conventional positive 87.8% plate 4-5 electrode plate Battery 11 Negative electrode Conventional positive 88.0% plate 4-6 electrode plate

As shown in Table 3, in comparison with a battery 1 using a conventional positive electrode plate and a conventional negative electrode plate, a battery using a current collector according to an embodiment of this application has good cycle life, and its cycle performance is equivalent to that of a conventional battery. In particular, for a battery made of a current collector including a protection layer, in comparison with a battery made of a current collector not including a protection layer, a capacity retention rate of the battery may be further increased, which indicates that reliability of the battery is higher.

6.3. Function of a Conductive Primer Layer in Improving Electrochemical Performance of a Battery

The following uses a positive electrode plate as an example to describe functions of factors such as the conductive primer layer and composition of the conductive primer layer in improving electrochemical performance of a battery. Table 4 shows specific composition and related parameters of batteries and electrode plates and current collectors that are used in the batteries in various embodiments and comparative examples. Table 5 shows a performance measurement result of each battery.

TABLE 4 Electrode plate Current collector Support layer Conductive layer Conductive Electrode active No. No. Material D1 Material D2 primer layer material layer Comparative Positive electrode PET 10 μm Al 1 μm / NCM333, 9.8 positive current collector 4 μm D50, and electrode plate 20 55 μm active material layer thickness Positive Positive electrode PET 10 μm Al 1 μm 10% conductive Same as electrode plate 21 current collector 4 carbon black, 90% above water-based polyacrylic acid, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 20% conductive Same as electrode plate 22 current collector 4 carbon black, 80% above water-based polyacrylic acid, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 50% conductive Same as electrode plate 23 current collector 4 carbon black, 50% above water-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 65% conductive Same as electrode plate 24 current collector 4 carbon black, 35% above water-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 80% conductive Same as electrode plate 25 current collector 4 carbon black, 20% above water-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 99% conductive Same as electrode plate 26 current collector 4 carbon black, 1% above water-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 65% conductive Same as electrode plate 27 current collector 4 carbon black, 35% above oil-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 80% conductive Same as electrode plate 28 current collector 4 carbon black, 20% above oil-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 32.5% conductive Same as electrode plate 29 current collector 4 carbon black, above 32.5% flake conductive graphite (0.05 μm D50), 35% water-based PVDF, and 1.5 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 65% conductive Same as electrode plate 30 current collector 4 carbon black, 35% above water-based PVDF, and 500 nm thickness Positive Positive electrode PET 10 μm Al 1 μm 65% conductive Same as electrode plate 31 current collector 4 carbon black, 35% above water-based PVDF, and 2 μm thickness Positive Positive electrode PET 10 μm Al 1 μm 65% conductive Same as electrode plate 32 current collector 4 carbon black. 35% above water-based PVDF, and 5 μm thickness

TABLE 5 Battery DCR growth No. Electrode plate rate Battery 20 Comparative positive Conventional negative  35% electrode plate 20 electrode plate Battery 21 Positive electrode Conventional negative 30.9% plate 21 electrode plate Battery 22 Positive electrode Conventional negative  29% plate 22 electrode plate Battery 23 Positive electrode Conventional negative  20% plate 23 electrode plate Battery 24 Positive electrode Conventional negative  15% plate 24 electrode plate Battery 25 Positive electrode Conventional negative 14.5% plate 25 electrode plate Battery 26 Positive electrode Conventional negative  14% plate 26 electrode plate Battery 27 Positive electrode Conventional negative 18.5% plate 27 electrode plate Battery 28 Positive electrode Conventional negative 18.2% plate 28 electrode plate Battery 29 Positive electrode Conventional negative 12.9% plate 29 electrode plate Battery 30 Positive electrode Conventional negative 15.5% plate 30 electrode plate Battery 31 Positive electrode Conventional negative 14.6% plate 31 electrode plate Battery 32 Positive electrode Conventional negative 14.1% plate 32 electrode plate

The following can be seen from the foregoing test data:

1. When a composite current collector with a thin conductive layer (that is, a comparative positive electrode plate 20 not including a conductive primer layer), because the composite current collector has disadvantages, for example, it has poorer conductivity than a conventional metal current collector and the conductive layer of the composite current collector may be easily damaged, there is great DCR in a battery and a cycle capacity retention rate is low. After a conductive primer layer is introduced, the conductive primer layer effectively repairs and establishes a conductive network between the current collector, the conductive primer layer, and an active substance to improve electronic transmission efficiency and reduce resistance of the current collector and an electrode active material layer, so that the DCR can be effectively reduced.

2. As content of a conductive agent in the conductive primer layer is increased (positive electrode plates 21 to 26), the DCR of the battery can be improved to a greater extent.

3. Given same composition, introduction of a water-based bonding agent can improve the DCR more apparently than an oil-based bonding agent (positive electrode plate 24 vs. positive electrode plate 27, and positive electrode plate 25 vs. positive electrode plate 28).

4. Because flake graphite may implement a buffer function, reduce damage to the conductive layer of the current collector in a compaction process, and reduce a crack by generating “horizontal sliding”, introduction of the flake graphite can further reduce the DCR of the battery (positive electrode plate 24 vs. positive electrode plate 29).

5. As a thickness of the conductive primer layer is increased (positive electrode plate 30 to positive electrode plate 32), the DCR of the battery can also be improved apparently. However, an excessively great thickness of the conductive primer layer is disadvantageous for improving energy density of the battery.

6.4. Function of Content of a Bonding Agent in an Electrode Active Material Layer in Improving Electrochemical Performance of a Battery.

When content of a bonding agent in an electrode active material layer is generally high, there is a strong bonding force between the active material layer and a primer layer, so that there is also a strong bonding force between an entire membrane layer (that is, a collective term of the active material layer and the conductive primer layer) and a composite current collector, and in an abnormal case such as nail penetration, the active material layer (or the membrane layer) can effectively wrap metal burrs generated in the conductive layer, to improve safety performance of the battery in nail penetration.

From a perspective of safety of the battery in nail penetration, the following uses a positive electrode plate as an example to describe a function of the content of the bonding agent in the electrode active material layer in improving electrochemical performance of the battery.

Positive electrode plates are prepared according to the method in the foregoing embodiment, but composition of slurries of positive electrode active material layers is adjusted. In this way, a plurality of positive electrode plates with different content of bonding agents in positive electrode active material layers are prepared. Refer to the following tables for specific composition of electrode plates.

TABLE 6 Electrode plate Current collector Conductive Electrode active No. No. Support layer Conductive layer primer layer material layer Positive Positive electrode PET 10 μm Al 1 μm 65% conductive NCM811, 6.5 μm electrode plate 33 current collector 4 carbon black, D50, 55 μm active 35% water-based material layer PVDF, and 1.5 thickness, and 0.5 μm thickness wt % conductive agent PVDF content Positive Positive electrode PET 10 μm Al 1 μm 65% conductive NCM811, 6.5 μm electrode plate 34 current collector 4 carbon black, D50, 55 μm active 35% water-based material layer PVDF, and 1.5 thickness, and 1 μm thickness wt % conductive agent PVDF content Positive Positive electrode PET 10 μm Al 1 μm 65% conductive NCM811, 6.5 μm electrode plate 35 current collector 4 carbon black, D50, 55 μm active 35% water-based material layer PVDF, and 1.5 thickness, and 2 μm thickness wt % conductive agent PVDF content Positive Positive electrode PET 10 μm Al 1 μm 65% conductive NCM811, 6.5 μm electrode plate 36 current collector 4 carbon black. D50, 55 μm active 35% water-based material layer PVDF. and 1.5 thickness, and 3 μm thickness wt % conductive agent PVDF content

Table 7 shows nail penetration test results when the foregoing different positive electrode plates are assembled into batteries. The results indicate that when content of a bonding agent in a positive electrode active material layer is higher, safety performance of a corresponding battery in nail penetration is higher. Preferably, the content of the bonding agent in the positive electrode active material layer is not less than 1 wt %, and more preferably, not less than 1.5 wt %.

TABLE 7 Battery Nail penetration No. Electrode plate test result Battery 33 Positive electrode Conventional negative 1 passed and 9 plate 33 electrode plate failed Battery 34 Positive electrode Conventional negative 6 passed and 4 plate 34 electrode plate failed Battery 35 Positive electrode Conventional negative All passed plate 35 electrode plate Battery 36 Positive electrode Conventional negative All passed plate 36 electrode plate

6.5. Surface Morphology of a Composite Current Collector

In a process of preparing a positive electrode plate 24, after cold pressing, a small sample is taken, and a surface of the positive electrode plate 24 is cleaned by using a piece of dust-free paper dipped in a DMC solvent, so that a surface of a composite current collector can be exposed. Then a surface morphology is observed by using a CCD microscope instrument. Refer to FIG. 13 for an observation diagram of the surface morphology. An obvious crack can be seen from FIG. 13. The crack is intrinsic to a surface of a conductive layer of the composite current collector, but such crack cannot be observed on a surface of a conventional metal current collector. When the conductive layer of the composite current collector is thin, a crack easily occurs when a pressure is applied to the conductive layer in a cold-pressing process during electrode plate machining. In this case, if there is a conductive primer layer, a conductive network between the current collector and an active substance may be effectively repaired and established to improve electronic transmission efficiency, and reduce resistance between the current collector and an electrode active material layer. Therefore, direct current resistance in a cell can be effectively reduced, power performance of the cell is improved, and it is ensured that phenomena such as great polarization and lithium precipitation do not easily occur in a long cycling process of the cell, that is, long-term reliability of the cell is effectively improved. Specifically, this is reflected as a significant slowdown of DCR growth and an improvement of battery performance. The foregoing observation result provides a possible theoretical explanation about a functional mechanism of the conductive primer layer, but it should be understood that this application is not limited to this specific theoretical explanation.

A person skilled in the art may understand that the foregoing shows an application example of an electrode plate in this application only by using a lithium battery as an example; however, the electrode plate in this application may also be applied to another type of battery or electrochemical apparatus, and a good technical effect of this application can still be achieved.

According to the disclosure and instruction of this specification, a person skilled in the art of this application may further make appropriate changes or modifications to the foregoing implementations. Therefore, this application is not limited to the foregoing disclosure and the described specific embodiments, and some changes or modifications to this application shall also fall within the protection scope of the claims of this application. In addition, although some specific terms are used in this specification, these terms are used only for ease of description, and do not constitute any limitation on this application. 

What is claimed is:
 1. An electrode plate, comprising a current collector and an electrode active material layer disposed on at least one surface of the current collector, wherein the current collector comprises a support layer and a conductive layer disposed on at least one surface of the support layer, a single-side thickness D2 of the conductive layer satisfies 30 nm≤D2≤3 μm, and a conductive primer layer comprising a conductive material and a bonding agent is further disposed between the current collector and the electrode active material layer.
 2. The electrode plate according to claim 1, wherein the conductive layer is a metal conductive layer, and a material of the metal conductive layer is one selected from at least one of aluminum, copper, nickel, titanium, silver, a nickel-copper alloy, and an aluminum-zirconium alloy; a material of the support layer is one selected from at least one of an insulating polymeric material, an insulating polymeric composite material, a conductive polymeric material, and a conductive polymeric composite material; the insulating polymeric material is selected from at least one of polyamide, polyterephthalate, polyimide, polyethylene, polypropylene, polystyrene, polyvinyl chloride, aramid fiber, polydiformylphenylenediamine, acrylonitrile-butadiene-styrene copolymer, polybutylene terephthalate, poly-p-phenylene terephthamide, poly(p-phenylene ether), polyoxymethylene, epoxy resin, phenolic resin, polytetrafluoroethylene, p-phenylene sulfide, polyvinylidene fluoride, silicon rubber, polycarbonate, cellulose and a derivative thereof, amylum and a derivative thereof, protein and a derivative thereof, polyvinyl alcohol and a crosslinking agent thereof, and polyethylene glycol and a crosslinking agent thereof; the insulating polymeric composite material is selected from a composite material formed by an insulating polymeric material and an inorganic material, wherein the inorganic material is one selected from at least one of a ceramic material, a glass material, and a ceramic composite material; the conductive polymeric material is selected from a polymeric polysulfur nitride material, or a doped conjugated polymeric material, for example, at least one of polypyrrole, polyacetylene, polyaniline, and polythiophene; the conductive polymeric composite material is selected from a composite material formed by an insulating polymeric material and a conductive material, wherein the conductive material is selected from at least one of a conductive carbon material, a metal material, and a composite conductive material, the conductive carbon material is selected from at least one of carbon black, a carbon nano-tube, graphite, acetylene black, and graphene, the metal material is selected from at least one of nickel, iron, copper, aluminum, or an alloy thereof, and the composite conductive material is selected from at least one of nickel-coated graphite powder and nickel-coated carbon fiber; and the material of the support layer is an insulating polymeric material or an insulating polymeric composite material.
 3. The electrode plate according to claim 1, wherein a thickness D1 of the support layer satisfies 1 μm≤D1≤30 μm; preferably, 1 μm≤D1≤15 μm; and/or a room-temperature Young's modulus E of the support layer satisfies 20 Gpa≥E≥4 Gpa; and/or there is a crack in the conductive layer.
 4. The electrode plate according to claim 1, wherein the single-side thickness D2 of the conductive layer satisfies 300 nm≤D2≤2 μm, and preferably, 500 nm≤D2≤1.5 μm.
 5. The electrode plate according to claim 1, wherein a protection layer is further disposed on one or two surfaces of the conductive layer; and a thickness D3 of the protection layer satisfies D3≤ 1/10 D2 and 1 nm≤D3≤200 nm, and preferably, 10 nm≤D3≤50 nm.
 6. The electrode plate according to claim 1, wherein a weight percentage of the conductive material is 10% to 99%, preferably, 20% to 80%, and more preferably 50% to 80%; and a weight percentage of the bonding agent is 1% to 90%, preferably, 20% to 80%, and more preferably 20% to 50%.
 7. The electrode plate according to claim 1, wherein: the conductive material is at least one of a conductive carbon material and a metal material, wherein the conductive carbon material is selected from at least one of zero-dimensional conductive carbon such as acetylene black or conductive carbon black, one-dimensional conductive carbon such as a carbon nano-tube, two-dimensional conductive carbon such as conductive graphite or graphene, and three-dimensional conductive carbon such as reduced graphene oxide, and the metal material is selected from at least one of aluminum powder, iron powder, and silver powder; the conductive material comprises a two-dimensional conductive carbon material, the two-dimensional conductive carbon material accounting for 1 wt % to 50 wt % of the conductive material, and preferably, a particle diameter D50 of the two-dimensional conductive carbon material is 0.01 μm to 0.1 μm; the bonding agent is selected from at least one of styrene butadiene rubber, oil-based polyvinylidene fluoride (PVDF), polyvinylidene fluoride copolymer, sodium carboxymethyl cellulose, polystyrene, polyacrylic acid, polytetrafluoroethylene, polyacrylonitrile, polyimide, water-based PVDF, polyurethane, polyvinyl alcohol, polyacrylate, polyacrylic-acid-polyacrylonitrile copolymer, and polyacrylate-polyacrylonitrile copolymer; and the bonding agent is a water-based bonding agent selected from at least one of water-based PVDF, polyacrylic acid, polyurethane, polyvinyl alcohol, polyacrylate, polyacrylic-acid-polyacrylonitrile copolymer, and polyacrylate-polyacrylonitrile copolymer.
 8. The electrode plate according to claim 1, wherein a single-side thickness H of the conductive primer layer is 0.1 μm to 5 μm; and preferably, a ratio of H to D2 is 0.5:1 to 5:1.
 9. The electrode plate according to claim 1, wherein the electrode active material layer comprises an electrode active material, a bonding agent, and a conductive agent; an average particle diameter D50 of the electrode active material is 5 μm to 15 μm; and content of the bonding agent in the electrode active material layer is not less than 1 wt % of a total weight of the electrode active material layer.
 10. A battery module, comprising a positive electrode plate, a negative electrode plate, a separator, and an electrolyte, wherein each of the positive electrode plate and the negative electrode plate comprises a current collector and an electrode active material layer disposed on at least one surface of the current collector, wherein the current collector comprises a support layer and a conductive layer disposed on at least one surface of the support layer, a single-side thickness D2 of the conductive layer satisfies 30 nm≤D2≤3 μm, and a conductive primer layer comprising a conductive material and a bonding agent is further disposed between the current collector and the electrode active material layer.
 11. The battery module according to claim 10, wherein the conductive layer is a metal conductive layer, and a material of the metal conductive layer is one selected from at least one of aluminum, copper, nickel, titanium, silver, a nickel-copper alloy, and an aluminum-zirconium alloy; a material of the support layer is selected from at least one of an insulating polymeric material, an insulating polymeric composite material, a conductive polymeric material, and a conductive polymeric composite material; the insulating polymeric material is selected from at least one of polyamide, polyterephthalate, polyimide, polyethylene, polypropylene, polystyrene, polyvinyl chloride, aramid fiber, polydiformylphenylenediamine, acrylonitrile-butadiene-styrene copolymer, polybutylene terephthalate, poly-p-phenylene terephthamide, poly(p-phenylene ether), polyoxymethylene, epoxy resin, phenolic resin, polytetrafluoroethylene, p-phenylene sulfide, polyvinylidene fluoride, silicon rubber, polycarbonate, cellulose and a derivative thereof, amylum and a derivative thereof, protein and a derivative thereof, polyvinyl alcohol and a crosslinking agent thereof, and polyethylene glycol and a crosslinking agent thereof; the insulating polymeric composite material is selected from a composite material formed by an insulating polymeric material and an inorganic material, wherein the inorganic material is one selected from at least one of a ceramic material, a glass material, and a ceramic composite material; the conductive polymeric material is selected from a polymeric polysulfur nitride material, or a doped conjugated polymeric material, for example, at least one of polypyrrole, polyacetylene, polyaniline, and polythiophene; the conductive polymeric composite material is selected from a composite material formed by an insulating polymeric material and a conductive material, wherein the conductive material is selected from at least one of a conductive carbon material, a metal material, and a composite conductive material, the conductive carbon material is selected from at least one of carbon black, a carbon nano-tube, graphite, acetylene black, and graphene, the metal material is selected from at least one of nickel, iron, copper, aluminum, or an alloy thereof, and the composite conductive material is selected from at least one of nickel-coated graphite powder and nickel-coated carbon fiber; and the material of the support layer is an insulating polymeric material or an insulating polymeric composite material.
 12. The battery module according to claim 10, wherein a thickness D1 of the support layer satisfies 1 μm≤D1≤30 μm; preferably, 1 μm≤D1≤15 μm; and/or a room-temperature Young's modulus E of the support layer satisfies 20 Gpa≥E≥4 Gpa; and/or there is a crack in the conductive layer.
 13. The battery module according to claim 10, wherein the single-side thickness D2 of the conductive layer satisfies 300 nm≤D2≤2 μm, and preferably, 500 nm≤D2≤1.5 μm.
 14. The battery module according to claim 10, wherein a protection layer is further disposed on one or two surfaces of the conductive layer; and a thickness D3 of the protection layer satisfies D3≤ 1/10 D2 and 1 nm≤D3≤200 nm, and preferably, 10 nm≤D3≤50 nm.
 15. The battery module according to claim 10, wherein a weight percentage of the conductive material is 10% to 99%, preferably, 20% to 80%, and more preferably 50% to 80%; and a weight percentage of the bonding agent is 1% to 90%, preferably, 20% to 80%, and more preferably 20% to 50%.
 16. The battery module according to claim 10, wherein: the conductive material is at least one of a conductive carbon material and a metal material, wherein the conductive carbon material is selected from at least one of zero-dimensional conductive carbon such as acetylene black or conductive carbon black, one-dimensional conductive carbon such as a carbon nano-tube, two-dimensional conductive carbon such as conductive graphite or graphene, and three-dimensional conductive carbon such as reduced graphene oxide, and the metal material is selected from at least one of aluminum powder, iron powder, and silver powder; the conductive material comprises a two-dimensional conductive carbon material, the two-dimensional conductive carbon material accounting for 1 wt % to 50 wt % of the conductive material, and preferably, a particle diameter D50 of the two-dimensional conductive carbon material is 0.01 μm to 0.1 μm; the bonding agent is selected from at least one of styrene butadiene rubber, oil-based polyvinylidene fluoride (PVDF), polyvinylidene fluoride copolymer, sodium carboxymethyl cellulose, polystyrene, polyacrylic acid, polytetrafluoroethylene, polyacrylonitrile, polyimide, water-based PVDF, polyurethane, polyvinyl alcohol, polyacrylate, polyacrylic-acid-polyacrylonitrile copolymer, and polyacrylate-polyacrylonitrile copolymer; and the bonding agent is a water-based bonding agent selected from at least one of water-based PVDF, polyacrylic acid, polyurethane, polyvinyl alcohol, polyacrylate, polyacrylic-acid-polyacrylonitrile copolymer, and polyacrylate-polyacrylonitrile copolymer.
 17. The battery module according to claim 10, wherein a single-side thickness H of the conductive primer layer is 0.1 μm to 5 μm; and preferably, a ratio of H to D2 is 0.5:1 to 5:1.
 18. The battery module according to claim 10, wherein the electrode active material layer comprises an electrode active material, a bonding agent, and a conductive agent; an average particle diameter D50 of the electrode active material is 5 μm to 15 μm; and content of the bonding agent in the electrode active material layer is not less than 1 wt % of a total weight of the electrode active material layer. 